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Prevalence of hyperhomocysteinaemia in a Chinese elderly population

Published online by Cambridge University Press:  18 March 2010

Quan-Gang Qu
Affiliation:
Institute of Reproductive and Child Health, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing 100191, People’s Republic of China
Jin-Ji Gao
Affiliation:
The Maternal and Child Health Care Hospital, Yuanshi County, Shijiazhuang City, Hebei Province, People’s Republic of China
Jian-Meng Liu*
Affiliation:
Institute of Reproductive and Child Health, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing 100191, People’s Republic of China
*
*Corresponding author: Email liujm@pku.edu.cn
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Abstract

Objective

To evaluate plasma homocysteine (Hcy) levels and prevalence rates of hyperhomocysteinaemia (HHCY) in elderly Chinese individuals.

Design

A cross-sectional study.

Setting

The study was conducted in 2006 in two counties from the north and the south of China.

Subjects

A total of 810 individuals aged 65–74 years were recruited. Demographic characteristics and lifestyle factors were assessed through questionnaire interviews and physical examination. Hcy and folate levels were measured in blood samples. The distribution of Hcy level was analysed according to Hcy-related factors.

Results

Northerners had higher Hcy levels (18·42 μmol/l) than southerners (10·20 μmol/l). Plasma Hcy was higher in men than in women and greater in smokers than in non-smokers. The prevalence rate of HHCY was 51·6 % in the north and 10·1 % in the south (P < 0·001). Hcy and plasma folate showed an inverse correlation (Spearman’s r = −0·44, P < 0·001; partial r = −0·229, P < 0·001). Region, gender, alcohol consumption and plasma folate were associated with HHCY among these elderly populations.

Conclusions

The results demonstrated that plasma Hcy levels and the prevalence rates of HHCY in Chinese elderly are considerably higher than those found in other countries, and substantial regional variations occur within China. The predominant determining factors of HHCY were region, gender, alcohol consumption and plasma folate. The elevated Hcy levels among elderly Chinese populations need to be decreased urgently.

Type
Research paper
Copyright
Copyright © The Authors 2010

Hyperhomocysteinaemia (HHCY) has been suggested as a risk factor for developing coronary artery disease, myocardial infarction and stroke(Reference Boushey, Beresford and Omenn1, 2). Epidemiological studies have documented that, in general populations, the most common risk factor for having HHCY is suboptimal or deficient vitamin (e.g. folate) status. Moreover, homocysteine (Hcy) levels also increase significantly with age and HHCY prevalence rates have been reported to be higher in the elderly than in other age groups(Reference Moustapha and Robinson3Reference McCully6). Thus, risk factors for HHCY may vary by life stage and nutritional background. Findings from younger age groups and populations with better nutritional status are unlikely to be applicable to the elderly. However, in view of the fact that both overall nutritional status and health status are associated with elevated risk of HHCY, the prevalence rates of HHCY among elderly populations should be evaluated.

Developed countries have carried out several large-scale population-based surveys to evaluate Hcy levels in the elderly, but there is a paucity of equivalent data from developing countries. In China, previous studies conducted among elderly individuals were mostly hospital-based, with limitations on study design, selection criteria and sample size. Cross-sectional surveys addressing the issue of differential relationships between Hcy levels and demographic characteristics and lifestyle factors among elderly Chinese populations (aged 65–74 years) are not yet available.

Thus the main purposes of the present study were to characterize the distribution of Hcy levels and identify determining factors associated with HHCY in Chinese individuals aged 65–74 years who live in northern and southern counties of China.

Materials and methods

Study design and population

We chose two counties as field sites: one (Yuanshi County, Hebei Province) in the north (near Beijing) and the other (Nanfeng County, Jiangsu Province) in the south (near Shanghai). In each region, two to four townships were selected so as to provide sufficient potentially eligible volunteers. Study participants were local residents and from the selected townships. An eligible person was aged 65–74 years in 2006. The first stage of the study involved providing local information and distributing informed consent forms to 1600 potentially eligible individuals in the two regions; 1200 (75 %) individuals agreed to participate in the recruitment process. Recruitment included questionnaire interviews, physical examinations and blood sample collection. Trained health workers were responsible for each recruitment step according to standard protocols. Researchers from Peking University were in charge of quality control. On the basis of data collected through recruitment, eligible participants were ascertained by researchers. Those who met any exclusion criterion could not participate in the study. Exclusion criteria included known CHD, hypertension, cancer, severe renal and liver diseases, diabetes, current use (≤6 months) of vitamins or other supplements, and taking medications known to interfere with folate metabolism (e.g. methotrexate). In our study, the main reasons for exclusion were hypertension (60 %), other chronic diseases (22 %) and vitamins taken in the past 6 months (4 %). Eventually, 810 (67·5 %) eligible individuals from 1200 consenting individuals were included in the study, with 405 subjects in each region. Within regions, the participants were distributed equivalently by gender and age groups (65–69 and 70–74 years old). Therefore, our analyses were based on 810 individuals with complete data.

Covariates

Demographic information and lifestyle factors were obtained by questionnaire interviews. BMI was calculated as kg/m2 from weight and height values. Current smoking was defined as smoking more than 1 cigarette/d for at least 1 month and still smoking. Individuals who were ex-smokers were counted as ‘ever smoking’ as a dichotomous variable. The rest were considered non-smokers. Alcohol consumption (including liquor, beer and wine) was classified into two categories: non-drinker and drinker.

Blood sample collection and homocysteine analyses

The 810 eligible participants were required to fast overnight before blood collection. Blood samples were drawn and collected in K3EDTA-containing Vacutainer tubes (Becton Dickinson, Franklin Lakes, NJ, USA), held at 4°C and centrifuged at 3000g for 15 min. Plasma and red blood cells were separated and frozen at –20°C within 1 h after collection. All specimens were transported on dry ice to the central laboratory at the Institute of Reproductive and Child Health, Peking University, and stored at −70°C until the assays were performed. Plasma folate concentrations were determined by a microbial assay (Lactobacillus casei) using a ninety-six-well plate as described by O’Broin and Kelleher(Reference O’Broin and Kelleher7). Plasma Hcy measurements were carried out by HPLC with fluorometric detection. In the laboratory, intra- and inter-assay CV across the full range of concentrations were 9 % for plasma folate and 8 % for Hcy. Repeat Hcy concentrations were measured for a sample of fifty individuals in our laboratory after all assessments were completed, and Spearman’s correlation coefficient between the before and after values for the same person was 0·86 (P < 0·001). In addition, the assessment of plasma folate was replicated for a sample of 100 individuals by the chemiluminescence method (Beckman Coulter, Fullerton, CA, USA) in a qualified laboratory. The Spearman’s correlation coefficient of two values performed by various methods was 0·93 (P < 0·01).

Individuals were classified as having HHCY if they had elevated Hcy concentration ≥16·0 μmol/l(Reference Ueland, Refsum and Stabler8). Individuals were classified as having plasma folate deficiency if they had plasma folate concentration ≤6·8 nmol/l(Reference Senti and Pilch9).

Ethical approval

The study was approved by the Institutional Review Boards of Peking University Health Science Center. All invited participants provided oral informed consent.

Statistical methods

Because the distributions of Hcy and plasma folate concentrations were positively skewed, natural logarithmic transformations were used to normalize their distributions. The geometric means as well as the 95 % confidence intervals were also determined. Student’s t test and one-way ANOVA were used to compare means. The significance of categorical variables was assessed by the χ 2 test or Fisher’s exact test. Logistic regression was used to estimate crude odds ratios of each variable alone in developing HHCY. Adjusted odds ratios were also determined after controlling for other factors (region, age, gender, BMI, occupation, educational background, hypertension, smoking and alcohol consumption). Spearman’s correlation coefficients and probabilities were calculated for the relationship between Hcy and plasma folate in continual quantitative variables. Subgroup analyses for certain risk factors were also conducted in females according to menopausal status and in males according to current smoking status.

The data were analysed with the SPSS statistical software package version 11·0 (SPSS, Beijing, China). All P values were two-sided at α level of 0·05.

Results

Selected characteristics of the study population are shown separately by region in Table 1. The demographic characteristics were similar between southerners and northerners. No significant differences were observed in current smoking, health status and medicine use.

Table 1 Characteristics of the study population by region: elderly Chinese individuals (n 810) aged 65–74 years, 2006

P value from t test for quantitative variables and χ 2 test for qualitative variables.

Compared with southerners, northerners had lower average BMI, less alcohol consumption, less smoking exposure (as indicated by ever smoking), and fewer had a family history of chronic disease. In addition, northerners were much more likely to have higher Hb levels and diastolic blood pressure than southerners, whereas their systolic blood pressures were similar.

The mean plasma folate levels were relatively low in this study population, but southerners appeared to be in better nutritional status than northerners, with significantly higher levels and corresponding lower deficiency rates.

Homocysteine concentrations

The distribution curves of plasma Hcy were skewed positively, but the curve for northerners had a very long tail towards high values (Fig. 1). Geometric means of Hcy according to demographic and lifestyle factors by region are shown in Table 2. Overall, the mean Hcy level of northerners was 18·42 μmol/l (95 % CI 17·40, 19·50 μmol/l) and nearly twice the level of southerners, i.e. 10·20 μmol/l (95 % CI 9·84, 10·58 μmol/l), thus being significantly higher in the north than in the south (P < 0·01).

Fig. 1 Distribution of plasma homocysteine concentrations among elderly Chinese individuals aged 65–74 years in the south (n 405; ——) and the north (n 405; - - - -) of China, 2006

Table 2 Plasma homocysteine levels (μmol/l) according to demographic and lifestyle factors by region: elderly Chinese individuals (n 810) aged 65–74 years, 2006

**P < 0·01.

Gender and smoking status differences in Hcy concentrations among both northerners and southerners were notable: men had higher Hcy levels than women, smokers higher than non-smokers. The absolute differences in Hcy concentrations between genders were of approximately similar magnitude as the corresponding absolute difference between smokers and non-smokers, and were greater than those for other factors. In each region, Hcy levels were not significantly influenced by other factors, except educational background in the south (P < 0·01, Table 2).

Prevalence rate of hyperhomocysteinaemia

The prevalence rate of HHCY was significantly higher in the north than in the south (P < 0·01), as shown in Table 3. Overall, HHCY (Hcy ≥ 16·0 μmol/l) was detected in 209 (51·6 %) northerners and forty-one (10·1 %) southerners, i.e. nearly five times as many in the north as in the south.

Table 3 Hyperhomocysteinaemia prevalence rates (%) according to demographic and lifestyle factors by region: elderly Chinese individuals (n 810) aged 65–74 years, 2006

*P < 0·05, **P < 0·01.

In each region, the prevalence rates of HHCY were observed to be higher in men than women and in smokers than non-smokers. However, the gender and smoking status differences were found to be significant only in the north (P < 0·01 for both), while neither of them was of significance in the south (P = 0·13). No statistically significant differences in HHCY prevalence rates were observed for other factors (Table 3).

We applied a logistic regression model to determine the association between each factor and HHCY, as shown in Table 4. Results showed that northerners had nine-fold higher odds of having HHCY than those living in the south. Men had a nearly 75 % increased risk of HHCY compared with women. In addition, those who were farmers, with higher education and those with hypertension were associated with a greater risk of HHCY to some extent. Interestingly, alcohol consumption showed protective effects for alcohol drinkers, with about 40 % (unadjusted OR = 0·58) or 50 % (adjusted OR = 0·50) reduced risk for elevated Hcy compared with non-drinkers. However, adjustment for the interactions between factors had no important effects on most of these associations except for region, gender and alcohol consumption.

Table 4 Crude and adjusted odds ratios, and their 95 % confidence intervals, of hyperhomocysteinaemia by demographic and lifestyle factors: elderly Chinese individuals (n 810) aged 65–74 years, 2006

*P < 0·05, **P < 0·01.

†Adjusted for region, gender, age, BMI, occupation, educational background, hypertension, current smoking and alcohol consumption. All variables used in the adjusted model were dichotomous variables.

Furthermore, subgroup analyses were conducted in male smokers (because very few women smoked in this population) and in postmenopausal women with HHCY. No significant associations were found in either analysis (data not shown).

Nutritional factors

Finally, we assessed the correlation between Hcy and plasma folate. Overall, plasma Hcy was inversely correlated with plasma folate (Spearman’s r = −0·44, P < 0·001) as expected. After adjusting for all other factors the inverse relationship still remained, resulting in a significant coefficient (partial correlation r = −0·229, P < 0·001). Among subjects with high Hcy levels, deficits of plasma folate were more prevalent in individuals from the north than in those from the south, 33 % v. 29 %, respectively. In contrast, 80 % of northerners and 38 % of southerners with low plasma folate showed high Hcy levels.

Discussion

High prevalence rate of hyperhomocysteinaemia

To our knowledge, the present study is the first to report data on Hcy concentrations by demographic and lifestyle factors in an elderly Chinese population. We found a high prevalence of HHCY in this population, in particular among the men (61 %) living in north China. Notable geographic and gender variations were observed for plasma Hcy concentrations among the study population, which may be the combined results of demographic and lifestyle factors, nutritional status and genetic backgrounds.

Gender, age and alcohol consumption

The largest population-based study, The Hordaland Homocysteine Study, demonstrated that Hcy concentrations increased with age and were higher in men than in women(Reference Nygard, Vollset and Refsum10). Detailed data on the Hcy levels of the elderly have also been reported from the third US National Health and Nutrition Examination Survey (NHANES III)(Reference Selhub, Jacques and Rosenberg11) and in other studies around the world(Reference Hoey, McNulty and Askin12Reference Bunout, Petermann and de la Maza24). Our study observed that Hcy levels were higher in men than in women, which is in agreement with the results of the Hordaland study. The male–female differences in Hcy concentrations probably result from the fact that renal cystathionine β-synthase activity is significantly lower in men than women, leading to higher Hcy levels by decreased conversion of Hcy to cysteine in the transsulfuration pathway(Reference Vitvitsky, Prudova and Stabler25). However, we did not find significant differences in Hcy concentrations between the two age groups (65–69 v. 70–74 years old), perhaps because the age span was smaller than 10 years. Our sample size was large enough that we can exclude the possibility of lacking power for non-significant differences. Additionally, our data confirmed the inverse association between Hcy levels and alcohol consumption reported by the Caerphilly cohort study(Reference Ubbink, Fehily and Pickering26). The possible explanations include, on the one hand, that the predominant type of alcoholic beverage (i.e. beer) consumed contains folate and that drinkers were likely to consume more food rich in folate (e.g. meat), on the other. These may indirectly improve folate status and decrease Hcy levels.

Regional variations

Overall, the south–north differences observed among the Chinese elderly population are consistent with previous published results from other younger populations. However, it is notable that the absolute prevalence rates of HHCY and the differences in Hcy levels between the two regions were more distinct in the elderly. The larger regional disparities could be explained, in part, by increasing age and different eating habits in the two regions. Moreover, genetic polymorphisms may be another essential factor. It has been reported that persons with the 5,10-methylenetetrahydrofolate reductase (MTHFR) 677-TT genotype have a 25·7 % higher Hcy concentration than those with the 677-CC genotype(Reference Yang, Botto and Gallagher27). Furthermore, several studies have pointed out that northerners have higher TT genotype frequency than southerners(Reference Chu, Huang and Kuang28, Reference Wilcken, Bamforth and Li29). Therefore, the MTHFR C677T polymorphism may explain, in part, the higher prevalence of HHCY in the north.

In addition, low plasma folate status might account for portions of these variations(Reference Joosten, Pelemans and Devos30). Individuals with elevated Hcy concentrations in our study also had low plasma folate concentrations and higher prevalence of deficits, with 10·06 nmol/l and 31·0 % in the north v. 14·17 nmol/l and 7·7 % in the south. We also found that a negative correlation between plasma folate levels and Hcy concentrations existed independent of other demographic and lifestyles factors, suggesting that plasma folate might be an important nutritional factor affecting Hcy levels in the two regions.

Comparison of hyperhomocysteinaemia prevalence between elderly populations in China and developed countries

The NHANES III study (1991–1994) defined HHCY as Hcy level higher than 11·4 μmol/l in male and 10·4 μmol/l in female populations who had good nutritional status and normal renal functioning(Reference Selhub, Jacques and Rosenberg11). On the basis of these criteria, the prevalence of HHCY in our study was converted into 83·7 % in the north and 34·3 % in the south. These high prevalence rates are twice those in Americans (≥60 years old), which are 43·2 % and 46·5 % for men and women, respectively. Since 1998, food fortification with folic acid has been implemented in the USA. The latest NHANES study showed that the average Hcy levels of the US population have declined by 8–10 % in men and by 3–13 % in women. Similarly, Hcy levels of the elderly have changed from 12·5 μmol/l before to 9·8 μmol/l after fortification(Reference Ganji and Kafai31, Reference Pfeiffer, Osterloh and Kennedy-Stephenson32). These findings suggest that even compared with the American elderly population living 20 years ago, the prevalence of HHCY among Chinese elderly is nearly two times greater, and might be much higher than the current levels of the American elderly.

In a cohort of elderly survivors from the Framingham study population, mean Hcy concentration was 11·9 μmol/l; values higher than 14 μmol/l were detected in 29·3 % of the subjects(Reference Selhub, Jacques and Wilson33). Under these criteria, our study found 63·7 % of northerners and 16·3 % of southerners had high Hcy levels.

Recently, a community-based prospective cohort study in Taiwan evaluated the cut-off point of Hcy for predicting risk of vascular diseases and death. Hcy levels were found to be statistically significantly related to cardiovascular events and all-cause deaths, with the best cut-off values being 9·47 μmol/l and 11·84 μmol/l, respectively(Reference Sun, Chien and Hsu34). Nygard et al. previously pointed out that Hcy values ≤9 μmol/l were associated with the lowest mortality level in CVD patients(Reference Nygard, Nordrehaug and Refsum35). In our study, 91·1 % of northerners and 59·8 % of southerners were found to be at risk of vascular diseases and death when 9 μmol/l was adopted. This finding implies that the elevated Hcy levels among Chinese elderly populations need to be decreased urgently.

Besides CVD and death, Hcy levels have also been reported to be associated with an increased risk of Alzheimer’s disease(Reference Clarke, Smith and Jobst36, Reference McCaddon, Davies and Hudson37) and colon cancer(Reference Kato, Dnistrian and Schwartz38) in older individuals. Until ongoing and completed intervention trials with folate in patients with chronic diseases obtain a definite conclusion on the potential roles of HHCY in these diseases, the observed lifestyle–Hcy relationships may contribute to the understanding of the aetiology and to possible prevention of some of these clinical conditions.

One limitation of the present study was the cross-sectional design with blood samples collected only in winter. These made it impossible to evaluate the data in terms of cause-and-effect relationships and we were unable to determine the impact of seasonal factors on Hcy levels. Moreover, our study sample was not a random sample of all the local populations; but on account of the stabilization of the local elderly population as well as their similar dietary habits and lifestyle, they were fairly representative of the eligible target elderly population living in the two regions. However, our study provided strong evidence of a high level of Hcy and a high prevalence of HHCY with distinct regional variations. These data are particularly important in the case of elderly populations who have a high absolute risk of vascular disease, and for whom individualized interventions with folate should be of most benefit.

Acknowledgements

Sources of funding: The study was supported by the National Nature Science Foundation, People’s Republic of China (Grant No. 30572071 and 30471486). The work of Q.Q. was supported by funds from Peking University Health Science Center, Beijing, People’s Republic of China (Grant No. BMU20090464-123). Conflict of interest declaration: The authors declare that there are no conflicts of interest. Author contributions: Q.-G.Q. conceptualized the paper, prepared data, conducted the statistical analysis, drafted and edited the manuscript. J.-J.G. was responsible for the field sites and data collection. J.-M.L. was the project leader, responsible for design, general coordination and supervision. Acknowledgements: We are deeply indebted to every health worker who participated in the survey for attending training sessions and collecting data, and to those participants from our two field sites for their devotion to the study.

References

1. Boushey, CJ, Beresford, SA, Omenn, GS et al. (1995) A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes. JAMA 274, 10491057.CrossRefGoogle ScholarPubMed
2. Homocysteine Studies Collaboration (2002) Homocysteine and risk of ischemic heart disease and stroke: a meta-analysis. JAMA 288, 20152022.CrossRefGoogle Scholar
3. Moustapha, A & Robinson, K (1998) High plasma homocysteine: a risk factor for vascular disease in the elderly. Coron Artery Dis 9, 725730.CrossRefGoogle ScholarPubMed
4. Kannel, WB (1997) Cardiovascular risk factors in the elderly. Coron Artery Dis 8, 565575.Google ScholarPubMed
5. Bates, CJ, Schneede, J, Mishra, G et al. (2003) Relationship between methylmalonic acid, homocysteine, vitamin B12 intake and status and socio-economic indices, in a subset of participants in the British National Diet and Nutrition Survey of people aged 65 y and over. Eur J Clin Nutr 57, 349357.CrossRefGoogle Scholar
6. McCully, KS (2007) Homocysteine, vitamins, and vascular disease prevention. Am J Clin Nutr 86, 1563S1568S.CrossRefGoogle ScholarPubMed
7. O’Broin, S & Kelleher, B (1992) Microbiological assay on microtitre plates of folate in serum and red cells. J Clin Pathol 45, 344347.CrossRefGoogle ScholarPubMed
8. Ueland, PM, Refsum, H, Stabler, SP et al. (1993) Total homocysteine in plasma or serum: methods and clinical applications. Clin Chem 39, 17641779.CrossRefGoogle ScholarPubMed
9. Senti, FR & Pilch, SM (1984) Assessment of the Folate Nutritional Status of the US Population Based on Data Collected in the Second National Health and Nutrition Examination Survey, 1976–1980. Bethesda, MD: Federation of American Societies for Experimental Biology.Google Scholar
10. Nygard, O, Vollset, SE, Refsum, H et al. (1995) Total plasma homocysteine and cardiovascular risk profile. The Hordaland Homocysteine Study. JAMA 274, 15261533.CrossRefGoogle ScholarPubMed
11. Selhub, J, Jacques, PF, Rosenberg, IH et al. (1999) Serum total homocysteine concentrations in the third National Health and Nutrition Examination Survey (1991–1994): population reference ranges and contribution of vitamin status to high serum concentrations. Ann Intern Med 131, 331339.CrossRefGoogle ScholarPubMed
12. Hoey, L, McNulty, H, Askin, N et al. (2007) Effect of a voluntary food fortification policy on folate, related B vitamin status, and homocysteine in healthy adults. Am J Clin Nutr 86, 14051413.CrossRefGoogle ScholarPubMed
13. Carlsson, CM, Pharo, LM, Aeschlimann, SE et al. (2004) Effects of multivitamins and low-dose folic acid supplements on flow-mediated vasodilation and plasma homocysteine levels in older adults. Am Heart J 148, E11.CrossRefGoogle ScholarPubMed
14. Gunstad, J, Bausserman, L, Paul, RH et al. (2006) C-reactive protein, but not homocysteine, is related to cognitive dysfunction in older adults with cardiovascular disease. J Clin Neurosci 13, 540546.CrossRefGoogle Scholar
15. Sutton-Tyrrell, K, Bostom, A, Selhub, J et al. (1997) High homocysteine levels are independently related to isolated systolic hypertension in older adults. Circulation 96, 17451749.CrossRefGoogle ScholarPubMed
16. Lim, HS & Heo, YR (2002) Plasma total homocysteine, folate, and vitamin B12 status in Korean adults. J Nutr Sci Vitaminol (Tokyo) 48, 290297.CrossRefGoogle ScholarPubMed
17. Hambaba, L, Abdessemed, S, Yahia, M et al. (2008) [Relationship between hyperhomocysteinemia and C677T polymorphism of methylene tetrahydrofolate reductase gene in a healthy Algerian population]. Ann Biol Clin (Paris) 66, 637641.Google Scholar
18. Fakhrzadeh, H, Ghotbi, S, Pourebrahim, R et al. (2006) Total plasma homocysteine, folate, and vitamin B12 status in healthy Iranian adults: the Tehran homocysteine survey (2003–2004)/a cross-sectional population based study. BMC Public Health 6, 29.CrossRefGoogle ScholarPubMed
19. van Oort, FV, Melse-Boonstra, A, Brouwer, IA et al. (2003) Folic acid and reduction of plasma homocysteine concentrations in older adults: a dose–response study. Am J Clin Nutr 77, 13181323.CrossRefGoogle ScholarPubMed
20. Schafer, JH, Glass, TA, Bolla, KI et al. (2005) Homocysteine and cognitive function in a population-based study of older adults. J Am Geriatr Soc 53, 381388.CrossRefGoogle Scholar
21. Koike, T, Kuzuya, M, Kanda, S et al. (2008) Raised homocysteine and low folate and vitamin B-12 concentrations predict cognitive decline in community-dwelling older Japanese adults. Clin Nutr 27, 865871.CrossRefGoogle ScholarPubMed
22. Kuo, HK, Liao, KC, Leveille, SG et al. (2007) Relationship of homocysteine levels to quadriceps strength, gait speed, and late-life disability in older adults. J Gerontol A Biol Sci Med Sci 62, 434439.CrossRefGoogle ScholarPubMed
23. Feng, L, Ng, TP, Chuah, L et al. (2006) Homocysteine, folate, and vitamin B-12 and cognitive performance in older Chinese adults: findings from the Singapore Longitudinal Ageing Study. Am J Clin Nutr 84, 15061512.CrossRefGoogle ScholarPubMed
24. Bunout, D, Petermann, M, de la Maza, P et al. (1998) [Serum homocysteine levels in healthy Chilean adults]. Rev Med Chil 126, 905910.Google ScholarPubMed
25. Vitvitsky, V, Prudova, A, Stabler, S et al. (2007) Testosterone regulation of renal cystathionine β-synthase: implications for sex-dependent differences in plasma homocysteine levels. Am J Physiol Renal Physiol 293, F594F600.CrossRefGoogle ScholarPubMed
26. Ubbink, JB, Fehily, AM, Pickering, J et al. (1998) Homocysteine and ischaemic heart disease in the Caerphilly cohort. Atherosclerosis 140, 349356.CrossRefGoogle ScholarPubMed
27. Yang, QH, Botto, LD, Gallagher, M et al. (2008) Prevalence and effects of gene–gene and gene–nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank. Am J Clin Nutr 88, 232246.CrossRefGoogle ScholarPubMed
28. Chu, JY, Huang, W, Kuang, SQ et al. (1998) Genetic relationship of populations in China. Proc Natl Acad Sci U S A 95, 1176311768.CrossRefGoogle ScholarPubMed
29. Wilcken, B, Bamforth, F, Li, Z et al. (2003) Geographical and ethnic variation of the 677C>T allele of 5,10-methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas worldwide. J Med Genet 40, 619625.CrossRefGoogle Scholar
30. Joosten, E, Pelemans, W, Devos, P et al. (1993) Cobalamin absorption and serum homocysteine and methylmalonic acid in elderly subjects with low serum cobalamin. Eur J Haematol 51, 2530.CrossRefGoogle ScholarPubMed
31. Ganji, V & Kafai, MR (2006) Population reference values for plasma total homocysteine concentrations in US adults after the fortification of cereals with folic acid. Am J Clin Nutr 84, 989994.Google ScholarPubMed
32. Pfeiffer, CM, Osterloh, JD, Kennedy-Stephenson, J et al. (2008) Trends in circulating concentrations of total homocysteine among US adolescents and adults: findings from the 1991–1994 and 1999–2004 National Health and Nutrition Examination Surveys. Clin Chem 54, 801813.CrossRefGoogle ScholarPubMed
33. Selhub, J, Jacques, PF, Wilson, PW et al. (1993) Vitamin status and intake as primary determinants of homocysteinemia in an elderly population. JAMA 270, 26932698.CrossRefGoogle Scholar
34. Sun, Y, Chien, KL, Hsu, HC et al. (2009) Use of serum homocysteine to predict stroke, coronary heart disease and death in ethnic Chinese. Circ J 73, 14231430.CrossRefGoogle ScholarPubMed
35. Nygard, O, Nordrehaug, JE, Refsum, H et al. (1997) Plasma homocysteine levels and mortality in patients with coronary artery disease. N Engl J Med 337, 230236.CrossRefGoogle ScholarPubMed
36. Clarke, R, Smith, AD, Jobst, KA et al. (1998) Folate, vitamin B12, and serum total homocysteine levels in confirmed Alzheimer disease. Arch Neurol 55, 14491455.CrossRefGoogle ScholarPubMed
37. McCaddon, A, Davies, G, Hudson, P et al. (1998) Total serum homocysteine in senile dementia of Alzheimer type. Int J Geriatr Psychiatry 13, 235239.3.0.CO;2-8>CrossRefGoogle ScholarPubMed
38. Kato, I, Dnistrian, AM, Schwartz, M et al. (1999) Serum folate, homocysteine and colorectal cancer risk in women: a nested case–control study. Br J Cancer 79, 19171922.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Characteristics of the study population by region: elderly Chinese individuals (n 810) aged 65–74 years, 2006

Figure 1

Fig. 1 Distribution of plasma homocysteine concentrations among elderly Chinese individuals aged 65–74 years in the south (n 405; ——) and the north (n 405; - - - -) of China, 2006

Figure 2

Table 2 Plasma homocysteine levels (μmol/l) according to demographic and lifestyle factors by region: elderly Chinese individuals (n 810) aged 65–74 years, 2006

Figure 3

Table 3 Hyperhomocysteinaemia prevalence rates (%) according to demographic and lifestyle factors by region: elderly Chinese individuals (n 810) aged 65–74 years, 2006

Figure 4

Table 4 Crude and adjusted odds ratios, and their 95 % confidence intervals, of hyperhomocysteinaemia by demographic and lifestyle factors: elderly Chinese individuals (n 810) aged 65–74 years, 2006